Target-CR: Targeted Health Coaching to Improve Physical Activity Post-Structured Cardiac Rehabilitation

Sponsor
Duke University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05773287
Collaborator
National Institute on Aging (NIA) (NIH)
30
2
12

Study Details

Study Description

Brief Summary

To identify factors and triggers influencing physical activity (PA) participation after structured cardiac rehabilitation (CR) among older adults who have enrolled in a center-based CR program, and compare the effects of a targeted health coaching intervention versus standard care immediately following structured CR on PA maintenance and functional fitness.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Targeted Health Coaching Group
  • Behavioral: Standard Care Group
N/A

Detailed Description

Approximately 800,000 individuals in the United States have a heart attack every year, with almost 1 in 4 of those individuals already having suffered a previous heart attack. Attending cardiac rehabilitation (CR) following a cardiovascular event improves cardiorespiratory fitness and health-related quality of life, as well as decreases the risk of future illness and death from heart disease. Unfortunately, once an individual finishes a CR program, continued participation in physical activity (PA) too often reverts to previous sedentary patterns, limiting beneficial health effects. Continued participation in PA post-CR is especially challenging among older adults - likely due to a lack of self-efficacy and confidence in their ability to perform PA due to either their age or other health conditions that make PA more challenging. However, the need to address other health conditions, in conjunction with the benefits of improved strength and mobility, makes continued PA participation following a structured CR program even more useful for older adults. Although individuals typically understand habitual participation in PA is good for their health, we poorly understand why some individuals successfully adhere to and maintain PA habits, while others succumb to barriers preventing them from maintaining the health benefits beyond CR. In addition to understanding factors and triggers influencing PA maintenance beyond CR, little research has developed or investigated interventions targeting this important transition period following structured CR programming to promote continued PA participation "at home". Therefore, this proposal aims to 1) identify factors and triggers influencing PA participation after a traditional 36-session CR program (Stage 0); and 2) test a targeted health coaching intervention using these identified triggers to optimize PA maintenance and mobility among older adults who completed a center-based CR program.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Targeted Health Coaching Intervention to Improve Physical Activity Maintenance and Mobility Post-Structured Cardiac Rehabilitation Programming Among Older Adults: A Pilot Study
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Targeted Health Coaching Group

Behavioral: Targeted Health Coaching Group
Participants in the THC group will receive an exercise prescription (steps/day) based on their last cardiac rehabilitation session exercise prescription. Participants will be provided a Garmin wearable device to track steps/day. Additionally, participants will partake in 6 virtual or in-person health coaching sessions lasting approximately 30-60 minutes in duration. These sessions will take place approximately every other week during the 3-month intervention period.

Placebo Comparator: Standard Care Group

Behavioral: Standard Care Group
Participants in the SC group will receive an exercise prescription (steps/day) based on their last cardiac rehabilitation session exercise prescription. Participants will be provided a Garmin wearable device to track steps/day. Additionally, participants will be provided with a single virtual or in-person education session, lasting approximately 30 minutes, at the beginning of the 3-month intervention period.

Outcome Measures

Primary Outcome Measures

  1. Change in Physical Activity Maintenance [Baseline, 3 months]

    Steps/day will be averaged across the intervention period

  2. Percent Change in Physical Activity Maintenance [Baseline, 3 months]

    Calculated as (steps/day completed) divided by (steps/day prescribed) times 100 and average across the study period

Secondary Outcome Measures

  1. Change in Senior Fitness Test Score (SFT) [Baseline, 3 months]

    Summed score from the six activities of the senior fitness test will be averaged. The six activities are: chair stand, arm curl, chair sit and reach, back scratch, 8-ft up and go, and 6-minute walk.

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Willingness to provide informed consent to participate in the Target-CR Study

  • Must be able to read and speak English well enough to provide informed consent and understand instructions

  • Age ≥60 years

  • Diagnosed with coronary heart disease

  • Of adequate clinical stability to allow study participation

  • Own a smartphone device for application download

Exclusion Criteria:
  • Planned relocation during the 3-month study period

  • Medical procedure scheduled within the 3-month study period that may limit physical activity (i.e., joint replacement)

  • Decompensated heart failure

  • Heart failure - New York Heart Association class IV

  • Severe valvular heart disease

  • Severe pulmonary hypertension

  • End-stage renal disease

  • Cardiac transplantation

  • Impairment from stroke, injury, or other medical condition that would prevent participation in the intervention

  • Dementia that would prevent participation in the intervention and following study protocols

  • Any other illnesses that, in the opinion of the local clinician, would negatively impact or mitigate participation in and completion of the protocol

  • Psychiatric illness (self-report and screening)

  • Hospitalization for any psychiatric condition within one year (self-report)

  • Integrative Health Coaching Mental Health Screening Questionnaire score >4 (screening)

  • Participation in an inpatient substance abuse rehabilitation program within one year

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Duke University
  • National Institute on Aging (NIA)

Investigators

  • Principal Investigator: William E. Kraus, MD, Duke University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Duke University
ClinicalTrials.gov Identifier:
NCT05773287
Other Study ID Numbers:
  • Pro00112929
  • 1P30AG064201-01
First Posted:
Mar 17, 2023
Last Update Posted:
Mar 17, 2023
Last Verified:
Mar 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Mar 17, 2023